Medical Device Manufacturer · US , Wilmington , MA

Menicon U.S.A., Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Menicon U.S.A., Inc. Ophthalmic ✕

3 devices

1-3 of 3

Cleared May 19, 2000

Ophthalmic · 122d

Cleared Aug 22, 1997

MENICON SF-P AND MENICON Z RIGID GAS PERMEABLE CONTACT LENS

Ophthalmic · 53d

Cleared Mar 25, 1997

MENICON Z BIFOCAL DESIGN LENS/MENICON Z TRIFOCAL DESIGN LENS

Ophthalmic · 82d